Evidence map›Paper›PMID 41883704›Full record

ArticleNeurology. Genetics2026

Expanding the

Alessandra Rocco, Christian Laurini, Yuri Matteo Falzone, Silvia Calzavara, Ubaldo Del Carro, Stefano Carlo Previtali, Francesca Maltecca

Abstract read
In one paragraph

Article in Neurology. Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Alessandra RoccoMitochondrial Dysfunctions in Neurodegeneration Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID https://orcid.org/0009-0000-4696-2318
Christian LauriniUniversità Vita-Salute San Raffaele, Milan, Italy.ORCID https://orcid.org/0009-0008-6707-3104
Yuri Matteo FalzoneDepartment of Neurology, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID https://orcid.org/0000-0003-3233-1907
Silvia CalzavaraUOC Medical Genetics, Molecular Genetics and Cytogenetics, IRCCS San Raffaele Scientific Institute, Milan, Italy; and.ORCID https://orcid.org/0009-0000-2958-4394
Ubaldo Del CarroNeurophysiology Service, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID https://orcid.org/0000-0003-3301-5412
Stefano Carlo PrevitaliUniversità Vita-Salute San Raffaele, Milan, Italy.ORCID https://orcid.org/0000-0003-2546-4357
Francesca MalteccaMitochondrial Dysfunctions in Neurodegeneration Unit, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.ORCID https://orcid.org/0000-0001-8095-8208

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: The Methods: We performed clinical evaluation, genetic analyses, electrophysiology, and functional studies in 1 patient's fibroblasts. Results: In this study, we report a patient presenting with progressive symmetric distal muscle atrophy, weakness, Discussion: These findings suggest that

Identifiers

PMID41883704
PMCPMC13010279

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.